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We utilize synchrotron X-ray diffraction measurements, conducted inside a diamond anvil cell, to analyze the high-pressure stability of Mg/Nb multilayered nanocomposites of equal (1:1) and unequal (1:10) thickness ratios. At larger layer thicknesses, Mg in these nanocomposites exists in its traditional hexagonal close packed (hcp) structure, while below a critical layer thickness of 7–8 nm, the Mg structure is found to transform into an interface strain-induced metastable pseudomorphic body center cubic (bcc) crystal structure. The hcp Mg present in the larger layer thicknesses exhibits an hcp-to-bcc phase transformation at pressures greater than 44 GPa, and this pressure value is found to vary between the equal and unequal Mg/Nb nanocomposite thickness ratios. On the other hand, the pseudomorphic bcc Mg structure is stable up to pressures of 60 GPa. Additionally, the compressibility of the pseudomorphic bcc Mg structure under pressure is shown to be fundamentally different from the bulk (nonlaminated) bcc Mg structure formed under high pressures. These results indicate that interface strain engineering, and an appropriate choice of the adjacent layer material, might be a viable pathway for tuning the structure and properties of the pseudomorphic bcc Mg structure. [ABSTRACT FROM AUTHOR]

High-Pressure Collaborative Access Team (HPCAT) is a synchrotron-based facility located at the Advanced Photon Source (APS). With four online experimental stations and various offline capabilities, HPCAT is focused on providing synchrotron x-ray capabilities for high pressure and temperature research and supporting a broad user community. Overall, the array of online/offline capabilities is described, including some of the recent developments for remote user support and the concomitant impact of the current pandemic. General overview of work done at HPCAT and with a focus on some of the minerals relevant work and supporting capabilities is also discussed. With the impending APS-Upgrade (APS-U), there is a considerable effort within HPCAT to improve and add capabilities. These are summarized briefly for each of the end-stations. [ABSTRACT FROM AUTHOR]

The pressure-temperature (P-T) phase diagram of ammonium nitrate (AN) [NH4NO3] has been determined using synchrotron x-ray diffraction (XRD) and Raman spectroscopy measurements. Phase boundaries were established by characterizing phase transitions to the high temperature polymorphs during multiple P-T measurements using both XRD and Raman spectroscopy measurements. At room temperature, the ambient pressure orthorhombic (Pmmn) AN-IV phase was stable up to 45 GPa and no phase transitions were observed. AN-IV phase was also observed to be stable in a large P-T phase space. The phase boundaries are steep with a small phase stability regime for high temperature phases. A P-V-T equation of state based on a high temperature Birch-Murnaghan formalism was obtained by simultaneously fitting the P-V isotherms at 298, 325, 446, and 467 K, thermal expansion data at 1 bar, and volumes from P-T ramping experiments. Anomalous thermal expansion behavior of AN was observed at high pressure with a modest negative thermal expansion in the 3-11 GPa range for temperatures up to 467 K. The role of vibrational anharmonicity in this anomalous thermal expansion behavior has been established using high P-T Raman spectroscopy. [ABSTRACT FROM AUTHOR]

High pressure infrared (IR) measurements of the insensitive explosive, 1,1-diamino-2,2-dinitroethylene (DADNE or FOX-7), have been performed in the far- and mid-IR spectral regions up to ∼28 GPa using a synchrotron source. Petroleum jelly and KBr were employed as the pressurizing media for the far- and mid-IR experiments, respectively. In both experiments, IR spectra were collected at various pressures both in compression and decompression to determine reversibility under pressure cycling. There is evidence for at least two and possibly three phase transitions in the samples at pressures near 2, 5, and10 GPa, respectively. In the high frequency region (∼3000-3300 cm-1), the NH2 symmetric and antisymmetric vibrational modes soften with increasing pressure, suggesting strengthening intermolecular hydrogen bonding, and then stiffen with further pressure increase. At higher pressures (above 5 GPa), we suspect progressive flattening of the zig zag structure characteristic of the α phase occurs, which was observed in the low temperature, quenched γ phase. FOX-7 was also observed to survive pressure cycling up to 28 GPa contrary to earlier reports of pressure-induced molecular decomposition. [ABSTRACT FROM AUTHOR]

Synchrotron X-ray radiation Laue diffraction is a widely used diagnostic technique for characterizing the microstructure of materials. An exciting feature of this technique is that comparable numbers of reflections can be measured several orders of magnitude faster than using monochromatic methods. This makes polychromatic beam diffraction a powerful tool for time-resolved microstructural studies, critical for understanding pressure-induced phase transition mechanisms, by in situ and in operando measurements. The current status of this technique, including experimental routines and data analysis, is presented along with some case studies. The new experimental setup at the High-Pressure Collaborative Access Team (HPCAT) facility at the Advanced Photon Source, specifically dedicated for in situ and in operando microstructural studies by Laue diffraction under high pressure, is presented. [ABSTRACT FROM AUTHOR]